Title : Sodium butyrate induces autophagy in colorectal cancer cells through LKB1/AMPK signaling.

Pub. Date : 2019 Feb

PMID : 30362049






4 Functional Relationships(s)
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Protein Name
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1 NaB treatment increased the formation of autolysosome and expression of phosphorylated liver kinase B1 (LKB1), AMP-activated protein kinase (AMPK), and acetyl-CoA carboxylase (ACC). nab protein kinase AMP-activated catalytic subunit alpha 1 Homo sapiens
2 NaB treatment increased the formation of autolysosome and expression of phosphorylated liver kinase B1 (LKB1), AMP-activated protein kinase (AMPK), and acetyl-CoA carboxylase (ACC). nab protein kinase AMP-activated catalytic subunit alpha 1 Homo sapiens
3 Treatment with compound C (an inhibitor of AMPK) and siRNA-mediated knockdown of AMPK and LKB1 significantly attenuated NaB-induced autophagy in CRC cells. nab protein kinase AMP-activated catalytic subunit alpha 1 Homo sapiens
4 Collectively, these findings indicated that LKB1 and AMPK are critical for NaB-mediated autophagy and may act as the novel targets for colorectal cancer therapy in the future. nab protein kinase AMP-activated catalytic subunit alpha 1 Homo sapiens